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Qa Documentation Associate I Job

Qa Documentation Associate I Job
Empresa:

(Confidencial)


Lugar:

Heredia

Detalles de la oferta

Additional Locations: Purpose and Passion - Comprehensive Benefits - Life:Work Integration - Community - Career Growth

At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we're solving some of the most important healthcare industry challenges. Together, we're one global team committed to making a difference in people's lives around the world. This is a place where you can find a career with meaningful purpose-improving lives through your life's work.

About the role

:Manage Documentation Center activities. Assure the BSC Costa Rica Documentation Center proceeds effectively and efficiently as per its functions, satisfying internal and external clients? needs, as well as local and corporate requirements related to documentation processes.

Your responsibilities include:

:Efficiently organize, plan, lead and control Documentation Center activities.
:Assure documentation is available and that document changes and approvals are performed in a timely manner.
:Assure the implementation of new corporate requirements related to the Documentation System.
:Contact the Corporate Documentation Department and other sites if required.
:Control the PDM process in the site.
:He/she may perform SAP transactions as required.
:Oversee functions and responsibilities of Documentation Center personnel are satisfied.
:He/she may train employees on PDM.
:He/she may train employees on PDM.
:Contact the Corporate PDM Department.
:May perform functions and tasks assigned to a BPL of PDM for BSC Costa Rica.
:Process documentation changes in PDM.
:Provide the required support in the Documentation area for BSC Costa Rica users.
:Review, evaluate, approve and recommend changes to local procedures and other documents related to assuring compliance with Corporate and ISO requirements:
:Assist in global conference calls and documentation process meetings.
:Ensure use of current version of official documents.
:Maintain and comply with Boston Scientific?s Good Documentation Practices System.
:Provide guidance and training for his/her personnel; support his/her subordinates in reaching their position goals; motivate individuals to obtain results; and keep high quality personnel.
:Contribute to the development of the budget and monitor its use.
:Additional Responsibilities:
:BPL Functions: create: reset PDM passwords; generate PDM reports; act as a link between the GSP Team and site users; prioritize and submit continuous improvement requests for the GSP team; communicate GSP and PDM information to users; coordinate local PDM initiatives; follow up on global PDM initiatives in the site; manage the link between user groups/roles.

What were looking for:

:Bachelor: Engineering or administration
:Desirable experience: 2+
:English level: 70:79
:Microsoft office basic
:SAP

About us

As a global medical technology leader for more than 35 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you're looking to truly make a difference to people both around the world and around the corner, there's no better place to make it happen.

Requisition ID:437292

:ul


Fuente: Tiptopjob2_Xml

Requisitos


Conocimientos:
Qa Documentation Associate I Job
Empresa:

(Confidencial)


Lugar:

Heredia

Built at: 2024-04-26T15:12:49.757Z